Barnwell J W, Nichols M E, Rubinstein P
New York University Medical Center, Department of Medical and Molecular Parasitology, New York 10010.
J Exp Med. 1989 May 1;169(5):1795-802. doi: 10.1084/jem.169.5.1795.
A short-term in vitro culture system that allows for significant re-invasion of target erythrocytes by Plasmodium vivax was used to study the role of the Duffy blood group antigen as a ligand for merozoite invasion by this human malaria species. Using human Duffy-positive and -negative erythrocytes, various primate erythrocytes, enzymatic modification of erythrocytes, and mAb that defines a new Duffy determinant (Fy6) we conclude that the erythrocyte glycoprotein carrying Duffy determinants is required as a ligand for the invasion of human erythrocytes by P. vivax merozoites. Blockade of invasion by Fab fragments of the anti-Fy6 mAb equal to that of the intact molecule and the correlation of P. vivax susceptibility with the presence of the Fy6 determinant suggests this epitope or a nearby domain may be an active site on the Duffy glycoprotein. However, as for P. knowlesi, there is evidence that an alternate pathway for P. vivax invasion of simian erythrocytes may exist.
一种允许间日疟原虫对靶红细胞进行显著再侵袭的短期体外培养系统被用于研究达菲血型抗原作为这种人类疟原虫裂殖子侵袭配体的作用。使用人类达菲阳性和阴性红细胞、各种灵长类红细胞、红细胞的酶修饰以及定义新达菲决定簇(Fy6)的单克隆抗体,我们得出结论,携带达菲决定簇的红细胞糖蛋白是间日疟原虫裂殖子侵袭人类红细胞所需的配体。抗Fy6单克隆抗体的Fab片段对侵袭的阻断作用与完整分子相当,以及间日疟原虫易感性与Fy6决定簇的存在之间的相关性表明,这个表位或附近区域可能是达菲糖蛋白上的一个活性位点。然而,至于诺氏疟原虫,有证据表明间日疟原虫侵袭猿猴红细胞可能存在一条替代途径。